首页> 外文期刊>Biochemical Pharmacology >Effects of tiadenol and di-(2-ethylhexyl)phthalate on the metabolism of phosphatidylcholine and phosphatidylethanolamine in the liver of rats: comparison with clofibric acid.
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Effects of tiadenol and di-(2-ethylhexyl)phthalate on the metabolism of phosphatidylcholine and phosphatidylethanolamine in the liver of rats: comparison with clofibric acid.

机译:噻苯丁醇和邻苯二甲酸二(2-乙基己基)酯对大鼠肝脏磷脂酰胆碱和磷脂酰乙醇胺代谢的影响:与氯纤维酸比较。

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Metabolic changes induced by 2,2'-(decamethylenedithio)diethanol (tiadenol) and di-(2-ethylhexyl)phthalate (DEHP) in the biosynthesis of phosphatidylcholine (PtdCho) and phosphatidylethanolamine (PtdEtn) in rat liver were compared with changes induced by p-chlorophenoxyisobutyric acid (clofibric acid). Treatment of rats with either tiadenol or DEHP increased the hepatic contents of PtdCho and PtdEtn, as was observed with clofibric acid treatment. The administration of tiadenol, DEHP, or clofibric acid slightly, but significantly, increased, in common, the activity of CTP:phosphocholine cytidylyltransferase, a key enzyme for the synthesis de novo of PtdCho, and suppressed the activity of PtdEtn N-methyltransferase. With regard to the enzymes involved in the synthesis of PtdEtn, the three peroxisome proliferators enhanced the activity of phosphatidylserine (PtdSer) decarboxylase and markedly decreased the activity of CTP:phosphoethanolamine cytidylyltransferase. Treatment of rats with the three compounds markedly increased, in common, the content and the proportion of the molecular species of PtdCho containing oleic acid (18:1), but considerably decreased the proportion of the molecular species of PtdCho containing linoleic acid (18:2) in the liver, resulting in a striking decrease in the concentration of the molecular species of PtdCho containing 18:2 in the serum. The present study suggests that the administration of peroxisome proliferators to rats increases the contents of hepatic PtdCho and PtdEtn for hepatomegaly and proliferation of organelles by the same mechanism, irrespective of their chemical structures.
机译:比较了2,2'-(癸亚甲基二硫代)二乙醇(tiadenol)和邻苯二甲酸二-(2-乙基己基)酯(DEHP)诱导的大鼠肝脏磷脂酰胆碱(PtdCho)和磷脂酰乙醇胺(PtdEtn)生物合成中的代谢变化。对氯苯氧基异丁酸(氯纤维酸)。用噻胆醇或DEHP处理大鼠会增加PtdCho和PtdEtn的肝含量,如氯贝酸治疗所观察到的。噻丹醇,DEHP或氯纤维酸的施用略微但显着地共同提高了CTP:磷酸胆碱胞苷转移酶(PtdCho从头合成的关键酶)的活性,并抑制了PtdEtn N-甲基转移酶的活性。关于参与PtdEtn合成的酶,这三种过氧化物酶体增殖物增强了磷脂酰丝氨酸(PtdSer)脱羧酶的活性,并显着降低了CTP:磷酸乙醇胺胞嘧啶转移酶的活性。用这三种化合物治疗大鼠,通常明显增加了含有油酸的PtdCho分子种类的含量和比例(18:1),但是却大大降低了含有亚油酸的PtdCho分子种类的比例(18:1)。 2)在肝脏中,导致血清中含有18:2的PtdCho分子种类的浓度显着下降。本研究表明,给大鼠施用过氧化物酶体增生剂,无论其化学结构如何,均通过相同的机制增加了肝脏PtdCho和PtdEtn的肝肿大和细胞器增殖的含量。

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